一种传感神经听力损失,在TRIOBP基因中含有新型化合物异合体变异:一个病例报告
Jung Woo Rhim1, Dong-Kee Kim2, Ji Yoon Han1
1Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Heliyon
|September 19, 2024
概括
这项研究确定了TRIOBP基因中的新型化合物异合体变异,在儿科患者中引起自体逆向非综合征性聋-28 (DFNB28). 需要进一步的研究来理解TRIOBP.
科学领域:
- 遗传学和基因组学 遗传学和基因组学
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 分子生物学分子生物学
背景情况:
- 自体递归非综合征性聋-28 (DFNB28) 与TRIOBP基因的突变有关,TRIOBP基因编码了一个Trio和F-actin结合蛋白.
- DFNB28呈现为由于同位素或复合异位素突变而导致的前语感神经听力损失 (SNHL).
- 本报告详细介绍了一例小儿病例,该病例在TRIOBP基因中出现了新型化合物异合体变异.
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